Principal Statistician

PSI CRO; München; Vor Ort; EUR 60.000 - 80.000; Vollzeit

Zusammenfassung

A leading clinical research organization in Munich is seeking a biostatistics project lead to contribute to statistical activities related to global clinical trials. The ideal candidate will hold an MSc in Statistics and possess expert knowledge in SAS programming, statistical principles, and the CDISC ADaM standard. This role involves analyzing clinical trial data and leading project teams. Strong communication skills and full proficiency in English are required.

Qualifikationen

• Full working proficiency in English.
• Ability to apply advanced statistical techniques.

Aufgaben

• Act as a communication line for project teams on statistical questions.
• Conduct statistical analysis for clinical trials.
• Develop and review study protocols and statistical analysis plans.
• Prepare and attend internal and external study audits.

Kenntnisse

Expert knowledge of statistical principles

SAS programming

CDISC ADaM standard

Adaptive designs

Sample size calculation

Strong presentation skills

Ausbildung

MSc in Statistics or equivalent

Jobbeschreibung

Overview

Company Description: We are the company that cares – for our staff, for our clients, for our partners and for the quality of work we do. A dynamic, global company founded in 1995, we bring together more than 2,700 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them.

Job Description: You will contribute to statistical activities related to global clinical trials and work closely with international teams of statisticians, programmers and data managers, including the role of biostatistics project lead.

In this role, you will:

• Act as a communication line for project teams, clients, vendors and internal team on statistical questions
• Conduct statistical analysis for clinical trials including, interim analysis, final analysis, analysis for DSMBs/DMCs and PK analysis
• Develop and review study protocols, statistical analysis plans, analysis dataset specifications according to CDISC ADaM standard and other project-specific documents
• Review statistical deliverables such as tables, figures, listings and analysis datasets
• Conduct departmental induction course and project-specific training for statisticians and SAS programmers
• Prepare for and attend internal and external study audits pertinent to Statistics
• Participate in preparation of internal/external audits follow up
• Provide input to standard operating procedures and other Quality Systems Documents (QSDs) pertinent to activities of Biostatistics department
• Liaise with DM on statistical questions related to data issues
• Participate in bid defense and in kick-off meetings
• Lead teams of SAS programmers and/or statisticians on the project level

Qualifications

• MSc in Statistics or equivalent
• Full working proficiency in English
• Expert knowledge and understanding of the statistical principles, concepts, methods, and standards used in clinical research
• Expert knowledge and understanding of the SAS programming
• Expert knowledge and understanding of CDISC ADaM standard
• Expert knowledge and understanding of adaptive designs
• Expert knowledge and understanding of sample size calculation
• Expert knowledge and understanding of relevant regulations and guidelines (e.g. FDA, EMA, ICH)
• Ability to apply advanced statistical techniques in support of clinical research studies and to analyze, interpret, and draw conclusions from complex statistical information
• Ability to consult with clinical investigators, interpret research requirements, and determine statistical analysis strategies
• Strong presentation and communication skills

Please submit your CV in English.

Additional Information

Our mission is to be the best CRO in the world as measured by our employees, clients, sites, and vendors. Our recruitment process is easy and straightforward, and we’ll be there with you every step of the way.